CN105382712A - High-speed cutting resin grinding wheel and preparing method thereof - Google Patents

High-speed cutting resin grinding wheel and preparing method thereof Download PDF

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Publication number
CN105382712A
CN105382712A CN201510651529.4A CN201510651529A CN105382712A CN 105382712 A CN105382712 A CN 105382712A CN 201510651529 A CN201510651529 A CN 201510651529A CN 105382712 A CN105382712 A CN 105382712A
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hour
phenol
minute
mentioned
weight
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黄浩
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Wuhu Hongkun Auto Parts Co Ltd
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Wuhu Hongkun Auto Parts Co Ltd
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Priority to CN201510651529.4A priority Critical patent/CN105382712A/en
Publication of CN105382712A publication Critical patent/CN105382712A/en
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B24GRINDING; POLISHING
    • B24DTOOLS FOR GRINDING, BUFFING OR SHARPENING
    • B24D3/00Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents
    • B24D3/02Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents the constituent being used as bonding agent
    • B24D3/20Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents the constituent being used as bonding agent and being essentially organic
    • B24D3/28Resins or natural or synthetic macromolecular compounds
    • B24D3/285Reaction products obtained from aldehydes or ketones
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B24GRINDING; POLISHING
    • B24DTOOLS FOR GRINDING, BUFFING OR SHARPENING
    • B24D18/00Manufacture of grinding tools or other grinding devices, e.g. wheels, not otherwise provided for
    • B24D18/0009Manufacture of grinding tools or other grinding devices, e.g. wheels, not otherwise provided for using moulds or presses
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B24GRINDING; POLISHING
    • B24DTOOLS FOR GRINDING, BUFFING OR SHARPENING
    • B24D3/00Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents
    • B24D3/34Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents characterised by additives enhancing special physical properties, e.g. wear resistance, electric conductivity, self-cleaning properties
    • B24D3/342Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents characterised by additives enhancing special physical properties, e.g. wear resistance, electric conductivity, self-cleaning properties incorporated in the bonding agent
    • B24D3/344Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents characterised by additives enhancing special physical properties, e.g. wear resistance, electric conductivity, self-cleaning properties incorporated in the bonding agent the bonding agent being organic
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G16/00Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00
    • C08G16/02Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00 of aldehydes
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G16/00Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00
    • C08G16/02Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00 of aldehydes
    • C08G16/04Chemically modified polycondensates
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20Oxides; Hydroxides
    • C08K3/22Oxides; Hydroxides of metals
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/34Silicon-containing compounds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20Oxides; Hydroxides
    • C08K3/22Oxides; Hydroxides of metals
    • C08K2003/2227Oxides; Hydroxides of metals of aluminium

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • General Chemical & Material Sciences (AREA)
  • Polishing Bodies And Polishing Tools (AREA)
  • Manufacture Of Macromolecular Shaped Articles (AREA)

Abstract

The invention discloses a high-speed cutting resin grinding wheel. The high-speed cutting resin grinding wheel comprises, by weight, 410-500 parts of CBN abrasive, 70-100 parts of white corundum powder, 96-110 parts of 34-40% of formaldehyde solution, 5-7 parts of boric acid, 2-6 parts of hexamethylene tetramine, 13-20 parts of aniline, 2-3 parts of potassium oxide, 90-100 parts of phenol, 3.6-4 parts of sodium fluosilicate and 0.6-1 part of pentaerythritol. The high-speed cutting resin grinding wheel is particularly suitable for high-speed cutting, and the grinding efficiency is high.

Description

A kind of high-speed cutting resin wheel and preparation method thereof
Technical field
The present invention relates to emery wheel technical field, particularly relate to a kind of high-speed cutting resin wheel and preparation method thereof.
Background technology
Along with automobile, the improving constantly of aircraft uniform velocity, more strict to the requirement of the friction material such as transmission, braking, and matrix is exploitation and the emphasis of research as the important component part of friction material always.Phenolic resins, epoxy resin, butadiene-styrene rubber and polytetrafluoroethylene (PTFE) all can be used as the matrix of friction material, but epoxy resin, butadiene-styrene rubber and polytetrafluoroethylene (PTFE) limit its application in friction material due to poor anti-wear performance, heat resistance and bond performance.The advantage of phenolic resins in heat resistance, bond performance, mechanical property, moulding processability and cost etc., becomes the most frequently used adhesive matrix material of composite friction material.But the defects such as when pure phenolic resin exists that fragility is large, poor toughness, hardness are high, heat resistance is not enough, intensity is low and use noise is large, extreme influence Properties of Friction Materials, therefore, carrying out modification to phenolic resins is the effective ways improving its combination property.
Summary of the invention
The object of the invention is exactly the defect in order to make up prior art, provides a kind of high-speed cutting resin wheel and preparation method thereof.
The present invention is achieved by the following technical solutions:
A kind of high-speed cutting resin wheel, it is made up of the raw material of following weight parts:
CBN abrasive material 410-500, white alundum powder 70-100,35-40% formalin 96-110, boric acid 5-7, hexamethylenetetramine 2-6, aniline 13-20, potassium oxide 2-3, phenol 90-100, prodan 3.6-4, pentaerythrite 0.6-1.
A preparation method for described high-speed cutting resin wheel, comprises the following steps:
(1) above-mentioned white alundum powder is joined in the sodium hydroxide solution of 10-16mol/l and soak 1-2 hour, filter, wash, dry, mix with the 10-16% of above-mentioned prodan weight, 40-50 minute is calcined at 300-350 DEG C, naturally cool, mix with potassium oxide, ball milling is even, is white fused alumina abrasive material;
(2) remaining prodan is joined in 17-20 times of deionized water, stir;
(3) 70-75% of 68-75%, 35-40% formalin weight of above-mentioned phenol weight is mixed, stir, add NaOH, adjustment PH is 8-9, and raised temperature is 70-75 DEG C, insulated and stirred 1.6-2 hour, add boric acid, raised temperature is 110-120 DEG C, decompression dehydration 50-60 minute, add the absolute ethyl alcohol of mixed system weight 2-3%, stir, first at 80-90 DEG C, heat 8-10 hour, then at 110-115 DEG C, heat 8-9 hour, cooling, obtains boric acid phenolic resins;
(4) by above-mentioned hexamethylenetetramine, the mixing of boric acid phenolic resins, wear into fine powder, cross 160-200 mesh sieve, obtain boric acid phenol-formaldehyde resin powder;
(5) by remaining phenol, the mixing of 35-40% formalin, add mixed liquor weight 1-1.5 butanone doubly, stir, be heated to 80-85 DEG C, drip aniline, insulation reaction 4-6 hour at the temperature disclosed above after dropwising, heating decompression distillation to system temperature is 100-105 DEG C, cooling, obtains benzoxazine monomer;
(6) by above-mentioned boric acid phenol-formaldehyde resin powder, the mixing of benzoxazine monomer, join in compound weight 2-3 butanone doubly, stirring and dissolving, vacuum drying 2.6-3 hour at 76-80 DEG C, concentrated, be cured under following intensification system, described intensification system is: 80-90 DEG C, 50-60 minute; 100-110 DEG C, 100-120 minute; 130-140 DEG C, 40-50 minute are benzoxazine phenol-formaldehyde resin modified;
(7) benzoxazine phenol-formaldehyde resin modified is joined in the prodan aqueous solution in step (2), stir, drip the sulfuric acid of 96-98%, adjustment PH is 1-3, and raised temperature is 60-70 DEG C, insulation reaction 1-2 hour, be cooled to normal temperature, mix with pentaerythrite, above-mentioned white fused alumina abrasive material, stir 20-30 minute, dehydration, obtains premix abrasive material;
(8) mixed with each raw material of residue by above-mentioned premix abrasive material, hot-forming, described hot pressing temperature is 160-170 DEG C, pressure 39O-410T, hot pressing time are 30-32 minute, and in hot pressing, every 4-5 minute steam bleeding once;
(9) by above-mentioned hot-forming after resin grinding wheels thickness closed assembly according to demand get up, separate with sheet iron plate, put into the hardening furnace preset and harden, the intensification system of sclerosis is: 100-120 DEG C, 4-5 hour; 125-140 DEG C, 7-8 hour; 150-170 DEG C, 1-2 hour; 180-185 DEG C, 8-9 hour; Naturally cool after stopping heating, obtain described resin wheel.
Advantage of the present invention is:
Emery wheel of the present invention has good heat endurance, and this is owing to introducing benzoxazine resin in phenolic cure structure, and it is a kind of containing phenyl ring and the heteroatomic dicyclic compound of N, O, so heat endurance is strong;
Wheel hardness of the present invention is high, and this is owing to adding benzoxazine monomer, and in its hot pressing at emery wheel and hardening process, volatile substances is few, reduces the porosity of emery wheel, improves compactness and hardness;
Emery wheel revolving strength of the present invention is high, and this is that emery wheel after hardening volume contraction is little owing to adding benzoxazine monomer, decreases internal stress and micro-crack;
The present invention introduces boron at emery wheel in phenolic resins, improve the combination property of finished product, this is because phenolic resins is to connect phenyl ring by C-C key, and boron bakelite resin is by B-" key connects phenyl ring; wherein the bond energy of C-C is the bond energy of 347KJ/mol, B-O is 523KJ/mol, far above the bond energy of C-C; define the three-dimensional cross-linked structure of boracic, can significantly improve the heat resistance of emery wheel, instantaneous heat-resisting quantity, ablation resistance;
Resin wheel of the present invention is specially adapted to high-speed cutting use, and grinding efficiency is high.
Detailed description of the invention
A kind of high-speed cutting resin wheel, it is made up of the raw material of following weight parts:
CBN abrasive material 410, white alundum powder 70,35% formalin 96, boric acid 5, hexamethylenetetramine 2, aniline 13, potassium oxide 2, phenol 90, prodan 3.6, pentaerythrite 0.6.
A preparation method for described high-speed cutting resin wheel, comprises the following steps:
(1) above-mentioned white alundum powder joined in the sodium hydroxide solution of 10mol/l and soak 1 hour, filter, wash, dry, mix with 10% of above-mentioned prodan weight, calcine 40 minutes at 300 DEG C, naturally cool, mix with potassium oxide, ball milling is even, is white fused alumina abrasive material;
(2) remaining prodan is joined in 17 times of deionized waters, stir;
(3) mix 70% of 68%, 35% formalin weight of above-mentioned phenol weight, stir, add NaOH, regulate PH to be 8, raised temperature is 70 DEG C, insulated and stirred 1.6 hours, add boric acid, raised temperature is 110 DEG C, decompression dehydration 50 minutes, add the absolute ethyl alcohol of mixed system weight 2%, stir, first heat 8 hours at 80 DEG C, then heat 8 hours at 110 DEG C, cooling, obtains boric acid phenolic resins;
(4) by above-mentioned hexamethylenetetramine, the mixing of boric acid phenolic resins, wear into fine powder, cross 160 mesh sieves, obtain boric acid phenol-formaldehyde resin powder;
(5) by remaining phenol, 35% formalin mixing, add the butanone of mixed liquor weight 1 times, stir, be heated to 80 DEG C, drip aniline, insulation reaction 4 hours at the temperature disclosed above after dropwising, heating decompression distillation to system temperature is 100 DEG C, and cooling, obtains benzoxazine monomer;
(6) by above-mentioned boric acid phenol-formaldehyde resin powder, the mixing of benzoxazine monomer, join in the butanone of compound weight 2 times, stirring and dissolving, vacuum drying 2.6 hours at 76 DEG C, concentrated, be cured under following intensification system, described intensification system is: 80 DEG C, 50 minutes; 100 DEG C, 100 minutes; 130 DEG C, 40 minutes is benzoxazine phenol-formaldehyde resin modified;
(7) benzoxazine phenol-formaldehyde resin modified is joined in the prodan aqueous solution in step (2), stir, drip the sulfuric acid of 96%, regulate PH to be 1, raised temperature is 60 DEG C, insulation reaction 1 hour, be cooled to normal temperature, mix with pentaerythrite, above-mentioned white fused alumina abrasive material, stir 20 minutes, dehydration, obtains premix abrasive material;
(8) mixed with each raw material of residue by above-mentioned premix abrasive material, hot-forming, described hot pressing temperature is 160 DEG C, pressure 39OT, hot pressing time are 30 minutes, and in hot pressing, every 4 minutes steam bleedings once;
(9) by above-mentioned hot-forming after resin grinding wheels thickness closed assembly according to demand get up, separate with sheet iron plate, put into the hardening furnace preset and harden, the intensification system of sclerosis is: 100 DEG C, 4 hours; 125 DEG C, 7 hours; 150 DEG C, 1 hour; 180 DEG C, 8 hours; Naturally cool after stopping heating, obtain described resin wheel.
Performance test:
Heat decomposition temperature: >=420 DEG C;
Revolving strength 141m/s;
Abrasion test: with commercially available phenolic resins emery wheel and the emery wheel of the present invention of identical weight, same size, weight is 1kg, cut channel-section steel continuously in the same way respectively, emery wheel weight after commercially available phenol resin sand wheel cutting is 973g, weight after emery wheel cutting of the present invention is 984g, wear away little, durability is high.

Claims (2)

1. a high-speed cutting resin wheel, is characterized in that what it was made up of the raw material of following weight parts:
CBN abrasive material 410-500, white alundum powder 70-100,35-40% formalin 96-110, boric acid 5-7, hexamethylenetetramine 2-6, aniline 13-20, potassium oxide 2-3, phenol 90-100, prodan 3.6-4, pentaerythrite 0.6-1.
2. a preparation method for high-speed cutting resin wheel as claimed in claim 1, is characterized in that comprising the following steps:
(1) above-mentioned white alundum powder is joined in the sodium hydroxide solution of 10-16mol/l and soak 1-2 hour, filter, wash, dry, mix with the 10-16% of above-mentioned prodan weight, 40-50 minute is calcined at 300-350 DEG C, naturally cool, mix with potassium oxide, ball milling is even, is white fused alumina abrasive material;
(2) remaining prodan is joined in 17-20 times of deionized water, stir;
(3) 70-75% of 68-75%, 35-40% formalin weight of above-mentioned phenol weight is mixed, stir, add NaOH, adjustment PH is 8-9, and raised temperature is 70-75 DEG C, insulated and stirred 1.6-2 hour, add boric acid, raised temperature is 110-120 DEG C, decompression dehydration 50-60 minute, add the absolute ethyl alcohol of mixed system weight 2-3%, stir, first at 80-90 DEG C, heat 8-10 hour, then at 110-115 DEG C, heat 8-9 hour, cooling, obtains boric acid phenolic resins;
(4) by above-mentioned hexamethylenetetramine, the mixing of boric acid phenolic resins, wear into fine powder, cross 160-200 mesh sieve, obtain boric acid phenol-formaldehyde resin powder;
(5) by remaining phenol, the mixing of 35-40% formalin, add mixed liquor weight 1-1.5 butanone doubly, stir, be heated to 80-85 DEG C, drip aniline, insulation reaction 4-6 hour at the temperature disclosed above after dropwising, heating decompression distillation to system temperature is 100-105 DEG C, cooling, obtains benzoxazine monomer;
(6) by above-mentioned boric acid phenol-formaldehyde resin powder, the mixing of benzoxazine monomer, join in compound weight 2-3 butanone doubly, stirring and dissolving, vacuum drying 2.6-3 hour at 76-80 DEG C, concentrated, be cured under following intensification system, described intensification system is: 80-90 DEG C, 50-60 minute; 100-110 DEG C, 100-120 minute; 130-140 DEG C, 40-50 minute are benzoxazine phenol-formaldehyde resin modified;
(7) benzoxazine phenol-formaldehyde resin modified is joined in the prodan aqueous solution in step (2), stir, drip the sulfuric acid of 96-98%, adjustment PH is 1-3, and raised temperature is 60-70 DEG C, insulation reaction 1-2 hour, be cooled to normal temperature, mix with pentaerythrite, above-mentioned white fused alumina abrasive material, stir 20-30 minute, dehydration, obtains premix abrasive material;
(8) mixed with each raw material of residue by above-mentioned premix abrasive material, hot-forming, described hot pressing temperature is 160-170 DEG C, pressure 39O-410T, hot pressing time are 30-32 minute, and in hot pressing, every 4-5 minute steam bleeding once;
(9) by above-mentioned hot-forming after resin grinding wheels thickness closed assembly according to demand get up, separate with sheet iron plate, put into the hardening furnace preset and harden, the intensification system of sclerosis is: 100-120 DEG C, 4-5 hour; 125-140 DEG C, 7-8 hour; 150-170 DEG C, 1-2 hour; 180-185 DEG C, 8-9 hour; Naturally cool after stopping heating, obtain described resin wheel.
CN201510651529.4A 2015-10-09 2015-10-09 High-speed cutting resin grinding wheel and preparing method thereof Pending CN105382712A (en)

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106002653A (en) * 2016-05-25 2016-10-12 安徽砥钻砂轮有限公司 Anti-wear and high-hardness modified resin grinding wheel and preparation method thereof
CN106041762A (en) * 2016-05-25 2016-10-26 安徽砥钻砂轮有限公司 Heat-resistance and wear-resistant modified silane resin grinding wheel and preparation method thereof
CN106217274A (en) * 2016-08-10 2016-12-14 吴迪 A kind of preparation method of hexafluoropropylene oxide phenol-formaldehyde resin modified emery wheel

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1082565A (en) * 1993-09-08 1994-02-23 肖宏遥 Contain boron modified phenolic resin composite material of glass flake and preparation method thereof
CN1323869A (en) * 2001-06-11 2001-11-28 海盐华强树脂有限公司 Cold pressing process of preparing friction material by using phenolic resin as adhesive
US20110053478A1 (en) * 2008-03-21 2011-03-03 Saint-Gobain Centre De Recherches Et D'etudes Europeen Fused and coated silica grains
CN102814747A (en) * 2012-07-31 2012-12-12 安徽威铭耐磨材料有限公司 CBN (cubic boron nitride) resin grinding wheel and preparation method thereof
CN103465179A (en) * 2013-09-05 2013-12-25 宁波大华砂轮有限公司 Resin rough grinding wheel and preparation method thereof
CN104861650A (en) * 2015-06-10 2015-08-26 花秀兵 Heat-resistant benzoxazine resin and preparation method thereof

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1082565A (en) * 1993-09-08 1994-02-23 肖宏遥 Contain boron modified phenolic resin composite material of glass flake and preparation method thereof
CN1323869A (en) * 2001-06-11 2001-11-28 海盐华强树脂有限公司 Cold pressing process of preparing friction material by using phenolic resin as adhesive
US20110053478A1 (en) * 2008-03-21 2011-03-03 Saint-Gobain Centre De Recherches Et D'etudes Europeen Fused and coated silica grains
CN102814747A (en) * 2012-07-31 2012-12-12 安徽威铭耐磨材料有限公司 CBN (cubic boron nitride) resin grinding wheel and preparation method thereof
CN103465179A (en) * 2013-09-05 2013-12-25 宁波大华砂轮有限公司 Resin rough grinding wheel and preparation method thereof
CN104861650A (en) * 2015-06-10 2015-08-26 花秀兵 Heat-resistant benzoxazine resin and preparation method thereof

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106002653A (en) * 2016-05-25 2016-10-12 安徽砥钻砂轮有限公司 Anti-wear and high-hardness modified resin grinding wheel and preparation method thereof
CN106041762A (en) * 2016-05-25 2016-10-26 安徽砥钻砂轮有限公司 Heat-resistance and wear-resistant modified silane resin grinding wheel and preparation method thereof
CN106217274A (en) * 2016-08-10 2016-12-14 吴迪 A kind of preparation method of hexafluoropropylene oxide phenol-formaldehyde resin modified emery wheel
CN106217274B (en) * 2016-08-10 2018-06-05 唐山市名鲨五金磨具有限公司 A kind of preparation method of hexafluoropropylene oxide phenol-formaldehyde resin modified emery wheel

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